CHAPTER XII

THALATTOSAURIA

Millions of years before the first appearance of the mosasaurs in

geological history, another group of reptiles showing many curious

resemblances to them attempted a rather precarious existence in the

water. Its members survived long enough to acquire many structural

adaptations to a water life, long enough to become diversely modified,

but not long enough, apparently, to wander far from their birthplace,

not long enough to attain that security from their enemies and more

ambitious competitors, the early ichthyosaurs and plesiosaurs, to

insure them a long existence. They were only a partial success as water

reptiles.

It has been only within a few years that we have had any knowledge

whatever of them, and that knowledge is still very incomplete, too

incomplete to justify any attempt to picture them as living animals,

even though we take the liberties that some of our illustrators

of extinct animals feel warranted in assuming. The first known

specimens of these “sea-reptiles”—for that is the meaning of the word

Thalattosauria—were discovered and described by Professor J. C. Merriam

less than ten years ago, and all our knowledge of these animals is due

to the same author, who has studied attentively the known specimens,

all of which are preserved in the museum of the University of

California. The first discovered fragmentary specimens were confounded

with those of early ichthyosaurs, from the Upper Triassic rocks of

northern California with which they were associated. No specimen has

yet been found that is even approximately complete; some parts of the

skeleton are not yet known, even from fragmentary remains, and not till

other and more complete specimens have been found will it be possible

to determine the real form of the living animals or to decide what

their nearest relationships with other reptiles were. Professor Merriam

thinks that they were related most closely with the Rhynchocephalia

(p. 176) of which the _Sphenodon_, or tuatera, of New Zealand is the

only living representative, but whose direct genealogical history runs

back nearly or quite to the time in which the thalattosaurs lived. On

the other hand, there are so many resemblances to the mosasaurs shown

in the remains that have been discovered, that it is possible the

thalattosaurs were only a short-lived branch of the primitive lizards,

which we also know were in existence at the time when the thalattosaurs

lived. However, even though they resembled the mosasaurs, there could

have been no direct genealogical relationships between them, for it is

quite certain that the thalattosaurs very soon went out of existence,

leaving no descendants. But it matters little which were the land

forbears of the thalattosaurs; they present such distinct adaptations

to water life—characters all their own—that their ancestral kinship may

well be left to the future researches of the curious paleontologist.

For the present, at least, they may well be placed in an order

of reptiles all their own, as Professor Merriam has proposed—the

Thalattosauria.

[Illustration: FIG. 82.—Skull of _Thalattosaurus_. (After Merriam)]

No thalattosaurs were large animals. If they had the same proportions

between the lengths of head, body, and tail as the mosasaurs, none

exceeded seven feet in length, and they may have been even shorter,

though probably not much. The figure of the skull, as restored by

Professor Merriam, shows many striking aquatic adaptations, in the

elongated, pointed muzzle, in the large external nostrils, situated

far back toward the eyes, and in the well-ossified ring of bones

surrounding the eyeball. There is a parietal opening in the roof of

the skull, as in the modern lizards and tuatera; but it is not known

for certainty whether there were two openings on each side in the

roof of the skull, as in the modern tuatera. While this character may

seem trivial, it is really one of the most important in the reptilian

anatomy in determining the relationship and classification of reptiles.

The teeth are conical and pointed in the front end of the upper and

lower jaws, but farther back they are rounded, rugose, and obtuse, and

could have been used only for crushing hard objects, like mollusks,

crustaceans, etc. (Fig. 82). And not only was there a row of such teeth

on each jaw (only partly seen in the figure), but similar teeth covered

a large part of the palate. And the lower jaws, it is seen, are rather

massive.

The vertebrae were, of course, of the more primitive kind, that is,

with the ends concave, both in front and behind. It would have been

strange indeed were they of any other kind, since reptiles with

ball-and-socket joints to the vertebrae, that is, concave on one end

and convex on the other, as in nearly all living reptiles, did not come

into existence till long after the thalattosaurs had disappeared from

geological history; and it is also a curious fact that such vertebrae

appear to have originated only among animals crawling on land, so that

they would not have been a character acquired by the thalattosaurs

after descending into the water. It will be seen from the figure of

a dorsal vertebra that the rib was attached by a single articular

surface, almost exclusively to the body of the vertebra, quite like

those of all lizards, snakes, and mosasaurs, and unlike those of

other reptiles. This too may seem to be a trivial character to prove

relationships with the lizards, but it is a curious fact that no two

animals having different kinds of ribs are closely related to each

other. Possibly, however, this looser mode of attachment of the ribs

in the thalattosaurs was one of their peculiar adaptations to a water

life, and may not have been derived from their land ancestors.

[Illustration: FIG. 83.—Dorsal vertebra of _Thalattosaurus_. (After

Merriam.)]

[Illustration: FIG. 84.—_Thalattosaurus_: bones of front extremity:

_s_, scapula; _c_, coracoid; _h_, humerus; _r_, radius; _u_, ulna.

(After Merriam.)]

Of the limbs, only a few bones are known, but these are very

instructive. The arm bones, as shown in Fig. 84, are strikingly like

those of the mosasaurs, as will be seen by comparing the figure on p.

157. The humerus is a little more elongated than that of the mosasaurs,

more nearly like the mosasaurian femur. The shoulder-blade and the

coracoid are imperfectly ossified, as is seen from the figure—another

characteristic of aquatic life. What the fingers and toes were like

cannot be said; probably they were bound together by membrane, forming

swimming paddles similar to those of the mosasaurs. Some of the bones

referred to the pelvis are known, but it is not known whether they are

united to the spinal column by a sacrum, as in land animals. Nor is

anything certainly known of the hind leg or much of the tail. Since the

front legs show marked aquatic adaptations, it is altogether certain

that the hind legs will be found to be modified more or less, though

not so much modified as the front legs, because, as we have seen, the

front legs are always more specialized in aquatic animals than the

hind ones, even as the hind legs are more specialized than the front

ones in land animals. Possibly the hind legs will be found to be more

like those of the Thalattosuchia, as shown on p. 212, that is, partly

terrestrial in character. Doubtless the tail was long and flattened,

possibly with a terminal fin-like dilation, though this is less

probable.

As regards the habits and food of the thalattosaurs, no better summary

can be given than that of Professor Merriam, in his own words:

The remains of thalattosaurs are known only in purely marine

deposits containing little or no material of terrestrial

origin. They are associated with a fauna consisting of

numerous forms, both vertebrate and invertebrate, which

are not known to have existed away from marine areas. In

the structure of the skeleton we find the abbreviated and

broadened proximal segments of the limbs, the slender snout

with prehensile terminal teeth, and the median superior

nostrils, indicating a purely aquatic type. There can

scarcely be room for doubt that the thalattosaurs as a group

were typical marine forms. The larger and more specialized

species comprised in the genus _Thalattosaurus_ were

strictly natatory. They may have visited the shore, but,

like the plesiosaurs, were better fitted for swimming

than for crawling. Of the smaller _Nectosaurus_

we unfortunately do not know the limbs. They may have

been considerably less specialized, and the animal

to a correspondingly greater degree a shore-dweller.

_Nectosaurus_ is, however, found in the same deposits

with other forms and appears to be as common as the others;

so that it is safe to consider it as having passed the

greater part of its life away from the shore.

From what we know of the vertebral column of

_Thalattosaurus_ it appears that the animal had

a relatively short neck and a long dorsal region, the

proportions being nearly those in the vertebral column of

some mosasaurs. Only the anterior portion of the caudal

region is known. The slender, rounded neural spines with

well-developed articulating processes seen here are not

such as commonly appear in forms with a highly specialized

sculling tail, and it is hardly probable that a caudal fin

of large size was developed.

The anterior limbs evidently formed paddles of moderate

size. The posterior pair may have been larger, in

compensation for lack of a strong sculling tail. It is,

however, possible, that as in _Geosaurus_ (of the

thalattosuchian crocodiles) the hind limbs were not

typically natatory, and the distal end of the tail was

vertically expanded.

No specimens have yet been found which are well enough

preserved to show any remains of the stomach contents,

and we have no definite evidence concerning the food of

the thalattosaurs, more than is furnished by the general

structure of the animal. The character of the paddles, the

form of the skull, and the presence of slender prehensile

teeth in the terminal portions of the jaws would indicate

that they fed in part upon some swiftly moving prey which

was caught by a quick snap of the jaws, deglutition being

assisted by the curved teeth of the pterygoids. The heavy

vomerine and posterior mandibular teeth may have been used

for crushing the light shells of ammonites, which existed in

vast numbers in the same seas.

Water Reptiles of the Past and Present · 第 12 / 16 章